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Juvenile osteoporosis

Known as: IJO, Idiopathic juvenile osteoporosis, Osteoporosis, juvenile 
 
National Institutes of Health

Papers overview

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2010
2010
Osteoporosis-pseudoglioma syndrome (OPS; OMIM 259770) is an autosomal-recessive genetic disorder characterized by severe… Expand
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2006
2006
IntroductionIdiopathic Juvenile Osteoporosis (IJO), a disease of unknown etiology, manifests typically by pain, bone deformities… Expand
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Review
2005
Review
2005
Osteoporosis is increasingly being seen in young people. The primitive forms are relatively rare, but the secondary forms… Expand
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2004
2004
We report on an 8 years and 3 months old boy with severe idiopathic juvenile osteoporosis (IJO). Clinical features included… Expand
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2002
2002
We have previously shown that idiopathic juvenile osteoporosis (IJO) is characterized by a decreased cancellous bone volume and a… Expand
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2000
2000
Osteoporosis in childhood is uncommon, and it may be secondary to a spectrum of diverse conditions. When such causes have been… Expand
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2000
2000
Idiopathic juvenile osteoporosis (IJO), a rare cause of osteoporosis in children, is characterized by the occurrence of vertebral… Expand
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1988
1988
An 8-year-old boy with idiopathic juvenile osteoporosis and multiple fractures had three abnormalities of bone mineral metabolism… Expand
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1982
1982
Low plasma calcitriol (1,25-dihydroxycholecalciferol) and normal serum calcifediol (25-hydroxycholecalciferol) levels were noted… Expand
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1969
1969
Abstract Thiazide diuretic administration was followed within three to four days by symptomatic hypercalcemia (calcium level of… Expand
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